Literature DB >> 914635

The molecular defects of alpha-thalassemia in the Filipino.

A M Dozy, H Kabisch, J Baker, H M Koenig, S Kurachi, G Stamatoyannopoulos, D Todd, Y W Kan.   

Abstract

Molecular hybridization with synthetic radioactive DNA (cDNA) complementry to alpha globin mRNA sequences shows that, as in most other Southeast Asian populations, the alpha globin structural genes are deleted in Filipinos affected by the alpha-thalassemia syndromes. Thus, all 4 alpha-globin structural genes are deleted in homozygous alpha-thalassemia with hydrops fetalis, 3 and 2 structural genes are deleted in hemoglobin H disease and alpha-thalassemia-1 respectively.

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Year:  1977        PMID: 914635     DOI: 10.3109/03630267709003418

Source DB:  PubMed          Journal:  Hemoglobin        ISSN: 0363-0269            Impact factor:   0.849


  3 in total

1.  alpha-Thalassaemia in Sardinian infants.

Authors:  R Galanello; G Diana; M Furbetta; A Angius; M A Melis; C Rosatelli; A Cao
Journal:  J Med Genet       Date:  1980-10       Impact factor: 6.318

2.  Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation.

Authors:  Y W Kan; A M Dozy
Journal:  Proc Natl Acad Sci U S A       Date:  1978-11       Impact factor: 11.205

3.  Modification of hemoglobin H disease by sickle trait.

Authors:  K K Matthay; W C Mentzer; A M Dozy; Y W Kan; D F Bainton
Journal:  J Clin Invest       Date:  1979-10       Impact factor: 14.808

  3 in total

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